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Construction of Mycobacterium tuberculosis cdd knockout and evaluation of invasion and growth in macrophages
Cytidine deaminase (MtCDA), encoded by cdd gene (Rv3315c), is the only enzyme identified in nucleotide biosynthesis pathway of Mycobacterium tuberculosis that is able to recycle cytidine and deoxycytidine. An M. tuberculosis knockout strain for cdd gene was obtained by allelic replacement. Evaluatio...
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Published in: | Memórias do Instituto Oswaldo Cruz 2019-05, Vol.112 (11) |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Cytidine deaminase (MtCDA), encoded by cdd gene (Rv3315c), is the only
enzyme identified in nucleotide biosynthesis pathway of Mycobacterium
tuberculosis that is able to recycle cytidine and deoxycytidine. An M.
tuberculosis knockout strain for cdd gene was obtained by allelic
replacement. Evaluation of mRNA expression validated cdd deletion and
showed the absence of polar effect. MudPIT LC-MS/MS data indicated
thymidine phosphorylase expression was decreased in knockout and
complemented strains. The cdd disruption does not affect M.
tuberculosis growth both in Middlebrook 7H9 and in RAW 264.7 cells,
which indicates that cdd is not important for macrophage invasion and
virulence. |
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ISSN: | 1678-8060 |